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The cerebrospinal fluid in multiple sclerosis: far beyond the bands

机译:多发性硬化中的脑脊液:远远超出了乐队

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The cerebrospinal fluid analysis has been employed for supporting multiple sclerosis diagnosis and ruling out the differential diagnoses. The most classical findings reflect the inflammatory nature of the disease, including mild pleocytosis, mild protein increase, intrathecal synthesis of immunoglobulin G, and, most typically, the presence of oligoclonal bands. In recent years, new biomarkers have emerged in the context of multiple sclerosis. The search for new biomarkers reflect the need of a better evaluation of disease activity, disease progression, and treatment efficiency. A more refined evaluation of disease and therapy status can contribute to better therapeutic choices, particularly in escalation of therapies. This is very relevant taking into account the availability of a greater number of drugs for multiple sclerosis treatment in recent years. In this review, we critically evaluate the current literature regarding the most important cerebrospinal fluid biomarkers in multiple sclerosis. The determination of biomarkers levels, such as chemokine ligand 13, fetuin A, and mainly light neurofilament has shown promising results in the evaluation of this disease, providing information that along with clinical and neuroimaging data may contribute to better therapeutic decisions.
机译:脑脊液分析已被用于支持多发性硬化症诊断和排除鉴别诊断。最经典的发现反映出该疾病的炎性性质,包括轻度的胞吞作用,轻度的蛋白质增加,鞘内合成的免疫球蛋白G,最常见的是存在寡克隆带。近年来,在多发性硬化的背景下出现了新的生物标志物。寻找新的生物标志物反映了需要更好地评估疾病活动性,疾病进展和治疗效率。对疾病和治疗状态的更精细评估可以有助于更好的治疗选择,尤其是在治疗升级中。考虑到近年来越来越多的药物可用于多发性硬化症治疗,因此这非常相关。在这篇综述中,我们对多发性硬化症中最重要的脑脊液生物标志物的文献进行了严格评估。生物标志物水平(例如趋化因子配体13,胎球蛋白A和主要是轻神经丝)的测定在评估该疾病方面显示出令人鼓舞的结果,提供的信息包括临床和神经影像数据可能有助于更好的治疗决策。

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